Canonical Allele Identifier: CA2201615235

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362575G= , CM000678.2:g.1362575G=	GRCh38
NC_000016.9:g.1412576G= , CM000678.1:g.1412576G=	GRCh37
NC_000016.8:g.1352577G=	NCBI36
NG_016985.1:g.15677G=
NG_033129.1:g.57130C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.709-36G=
ENST00000529110.2:c.694-36G=	ENSP00000435349.2:n.694-36G=
ENST00000529957.6:n.668-36G=
ENST00000683366.1:c.*342-36G=	ENSP00000507283.1:n.*342-36G=
ENST00000683887.1:c.658-36G=	ENSP00000506886.1:n.658-36G=
ENST00000684100.1:n.604-36G=
ENST00000684126.1:n.708G=
ENST00000684688.1:n.1235-36G=
ENST00000204679.9:c.610-36G= MANE Select	ENSP00000204679.4:n.610-36G=
ENST00000204679.8:c.610-36G=	ENSP00000204679.4:n.610-36G=
ENST00000527076.1:n.1797G=
ENST00000527168.5:n.777-36G=
ENST00000529957.5:n.709-36G=
NM_032520.4:c.610-36G=	NP_115909.1:n.610-36G=
XM_017023782.1:c.658-36G=	XP_016879271.1:n.658-36G=
XM_017023783.1:c.250-36G=	XP_016879272.1:n.250-36G=
NM_032520.5:c.610-36G= MANE Select	NP_115909.1:n.610-36G=